Wordt geladen...
Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome
Increasing evidence has demonstrated that lung fluid absorption disorders might be an important cause of neonatal respiratory distress syndrome (RDS) by influencing gas exchange or surfactant function. The SCNN1A gene, which encodes the α-ENaC, might predispose infants to RDS. To explore whether the...
Bewaard in:
| Gepubliceerd in: | Sci Rep |
|---|---|
| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Nature Publishing Group
2015
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4661423/ https://ncbi.nlm.nih.gov/pubmed/26611714 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep17317 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|